Variant (rsID / SNP)
rs11068551
rs11068551 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to KSR2. Location: chromosome 12, position 118,020,115. The table records no clinical significance for this variant.
Reference-table entries
KSR2Not classified
- Variant type
- synonymous_variant
- Chromosome / position
- 12:118020115
- HGVS
- NM_173598.6,c.1221C>T,p.Leu407Leu
- Allele change
- Synonymous_L378L
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.